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1-4 of 4
Vorasuk Shotelersuk
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Journal Articles
A Novel GNAS Mutation Causing Isolated Infantile Cushing’s Syndrome
Available to PurchasePrapai Dejkhamron, Chupong Ittiwut, Hataitip TangNgam, Kanokkarn Sunkonkit, Rungrote Natesirinilkul, Kanya Suphapeetiporn, Vorasuk Shotelersuk
Journal:
Hormone Research in Paediatrics
Horm Res Paediatr (2020) 92 (3): 196–202.
Published Online: 30 July 2019
Journal Articles
Functional Characterization of Vasopressin Receptor 2 Mutations Causing Partial and Complete Congenital Nephrogenic Diabetes Insipidus in Thai Families
Available to PurchaseTaninee Sahakitrungruang, Meng Kian Tee, Natthakorn Rattanachartnarong, Vorasuk Shotelersuk, Kanya Suphapeetiporn, Walter L. Miller
Journal:
Hormone Research in Paediatrics
Horm Res Paediatr (2010) 73 (5): 349–354.
Published Online: 14 April 2010
Journal Articles
A Novel Germline Mutation, IVS4+1G>A, of the POU1F1 Gene Underlying Combined Pituitary Hormone Deficiency
Available to PurchaseThiti Snabboon, Wanee Plengpanich, Patinat Buranasupkajorn, Ratchada Khwanjaipanich, Padiporn Vasinanukorn, Sompongse Suwanwalaikorn, Weerapan Khovidhunkit, Vorasuk Shotelersuk
Journal:
Hormone Research in Paediatrics
Hormone Research (2007) 69 (1): 60–64.
Published Online: 04 December 2007
Journal Articles
A Girl with a Novel Splice Site Mutation in VDR Supports the Role of a Ligand-Independent VDR Function on Hair Cycling
Available to Purchase
Journal:
Hormone Research in Paediatrics
Hormone Research (2006) 66 (6): 273–276.
Published Online: 30 November 2006